Canonical Allele Identifier: CA555999452
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1490088438
gnomAD v2: 4-169086611-C-T
gnomAD v3: 4-168165460-C-T
gnomAD v4: 4-168165460-C-T
MyVariant Identifiers: chr4:g.169086611C>T (hg19) chr4:g.168165460C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165460C>T , CM000666.2:g.168165460C>T GRCh38
NC_000004.11:g.169086611C>T , CM000666.1:g.169086611C>T GRCh37
NC_000004.10:g.169323186C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+134C>T MANE Select ENSP00000352248.3:n.480+134C>T
ENST00000359299.7:c.480+134C>T ENSP00000352248.3:n.480+134C>T
ENST00000503003.1:n.86+134C>T
ENST00000507278.5:n.143+134C>T
ENST00000617524.1:c.477+134C>T ENSP00000483710.1:n.477+134C>T
NM_007193.4:c.480+134C>T NP_009124.2:n.480+134C>T
XM_011531571.1:c.540+134C>T XP_011529873.1:n.540+134C>T
XM_011531571.2:c.540+134C>T XP_011529873.1:n.540+134C>T
NM_007193.5:c.480+134C>T MANE Select NP_009124.2:n.480+134C>T
Search 100 bp 5'
Search 100 bp 3'